Synthesis of N-phenacyl Pyridines and N-phenacyl Piperidines
These N-substituted piperidines, because of their similarity in structure to the pressor amines, are expected to be physiologically active. By varying the position and size of the alkyl groups attached to the pyridine ring, difference in degree and type of physiological activity are likely.
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| Format: | Others |
| Language: | English |
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North Texas State Teachers College
1947
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| Online Access: | https://digital.library.unt.edu/ark:/67531/metadc798281/ |